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Visualizing long-range movement of the morphogen Xnr2 in the Xenopus embryo. , Williams PH., Curr Biol. November 9, 2004; 14 (21): 1916-23.
Negative regulation of Smad2 by PIASy is required for proper Xenopus mesoderm formation. , Daniels M., Development. November 1, 2004; 131 (22): 5613-26.
XSIP1 is essential for early neural gene expression and neural differentiation by suppression of BMP signaling. , Nitta KR., Dev Biol. November 1, 2004; 275 (1): 258-67.
A vertebrate crossveinless 2 homologue modulates BMP activity and neural crest cell migration. , Coles E., Development. November 1, 2004; 131 (21): 5309-17.
Cdc42 Effector Protein 2 ( XCEP2) is required for normal gastrulation and contributes to cellular adhesion in Xenopus laevis. , Nelson KK., BMC Dev Biol. October 8, 2004; 4 13.
Identification and characterization of Xenopus OMP25. , Inui M., Dev Growth Differ. October 1, 2004; 46 (5): 405-12.
R-Spondin2 is a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis. , Kazanskaya O., Dev Cell. October 1, 2004; 7 (4): 525-34.
Activin redux: specification of mesodermal pattern in Xenopus by graded concentrations of endogenous activin B. , Piepenburg O., Development. October 1, 2004; 131 (20): 4977-86.
Polarized distribution of mRNAs encoding a putative LDL receptor adaptor protein, xARH (autosomal recessive hypercholesterolemia) in Xenopus oocytes. , Zhou Y., Mech Dev. October 1, 2004; 121 (10): 1249-58.
A Xenopus tribbles orthologue is required for the progression of mitosis and for development of the nervous system. , Saka Y ., Dev Biol. September 15, 2004; 273 (2): 210-25.
Repression of nodal expression by maternal B1-type SOXs regulates germ layer formation in Xenopus and zebrafish. , Zhang C., Dev Biol. September 1, 2004; 273 (1): 23-37.
The role of Xenopus frizzled-8 in pronephric development. , Satow R., Biochem Biophys Res Commun. August 20, 2004; 321 (2): 487-94.
p120 catenin is required for morphogenetic movements involved in the formation of the eyes and the craniofacial skeleton in Xenopus. , Ciesiolka M., J Cell Sci. August 15, 2004; 117 (Pt 18): 4325-39.
Xenopus XsalF: anterior neuroectodermal specification by attenuating cellular responsiveness to Wnt signaling. , Onai T., Dev Cell. July 1, 2004; 7 (1): 95-106.
The Meis3 protein and retinoid signaling interact to pattern the Xenopus hindbrain. , Dibner C., Dev Biol. July 1, 2004; 271 (1): 75-86.
Activin-like signaling activates Notch signaling during mesodermal induction. , Abe T., Int J Dev Biol. June 1, 2004; 48 (4): 327-32.
The intracellular domain of X- Serrate-1 is cleaved and suppresses primary neurogenesis in Xenopus laevis. , Kiyota T., Mech Dev. June 1, 2004; 121 (6): 573-85.
Guidance of mesoderm cell migration in the Xenopus gastrula requires PDGF signaling. , Nagel M., Development. June 1, 2004; 131 (11): 2727-36.
Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus. , Kuroda H ., PLoS Biol. May 1, 2004; 2 (5): E92.
XIdax, an inhibitor of the canonical Wnt pathway, is required for anterior neural structure formation in Xenopus. , Michiue T ., Dev Dyn. May 1, 2004; 230 (1): 79-90.
Regulated gene expression of hyaluronan synthases during Xenopus laevis development. , Nardini M., Gene Expr Patterns. May 1, 2004; 4 (3): 303-8.
Xenopus MBD3 plays a crucial role in an early stage of development. , Iwano H., Dev Biol. April 15, 2004; 268 (2): 416-28.
ALK4 functions as a receptor for multiple TGF beta-related ligands to regulate left- right axis determination and mesoderm induction in Xenopus. , Chen Y ., Dev Biol. April 15, 2004; 268 (2): 280-94.
Vertebrate development requires ARVCF and p120 catenins and their interplay with RhoA and Rac. , Fang X., J Cell Biol. April 1, 2004; 165 (1): 87-98.
Ca(2+)(cyt) negatively regulates the initiation of oocyte maturation. , Sun L., J Cell Biol. April 1, 2004; 165 (1): 63-75.
Cytoplasmic and molecular reconstruction of Xenopus embryos: synergy of dorsalizing and endo-mesodermalizing determinants drives early axial patterning. , Katsumoto K., Development. March 1, 2004; 131 (5): 1135-44.
Cloning and developmental expression of MARK/ Par-1/ MELK-related protein kinase xMAK-V in Xenopus laevis. , Ruzov AS., Dev Genes Evol. March 1, 2004; 214 (3): 139-43.
Xvelo1 uses a novel 75-nucleotide signal sequence that drives vegetal localization along the late pathway in Xenopus oocytes. , Claussen M., Dev Biol. February 15, 2004; 266 (2): 270-84.
Lefty blocks a subset of TGFbeta signals by antagonizing EGF- CFC coreceptors. , Cheng SK., PLoS Biol. February 1, 2004; 2 (2): E30.
Morphogenesis during Xenopus gastrulation requires Wee1-mediated inhibition of cell proliferation. , Murakami MS., Development. February 1, 2004; 131 (3): 571-80.
Transcriptional regulation of the cardiac-specific MLC2 gene during Xenopus embryonic development. , Latinkic BV ., Development. February 1, 2004; 131 (3): 669-79.
Oocyte maturation in Xenopus laevis is blocked by the hormonal herbicide, 2,4-dichlorophenoxy acetic acid. , Stebbins-Boaz B., Mol Reprod Dev. February 1, 2004; 67 (2): 233-42.
Morphogenetic movements underlying eye field formation require interactions between the FGF and ephrinB1 signaling pathways. , Moore KB ., Dev Cell. January 1, 2004; 6 (1): 55-67.
Xenopus tropicalis nodal-related gene 3 regulates BMP signaling: an essential role for the pro-region. , Haramoto Y ., Dev Biol. January 1, 2004; 265 (1): 155-68.
Identification of BOIP, a novel cDNA highly expressed during spermatogenesis that encodes a protein interacting with the orange domain of the hairy-related transcription factor HRT1/ Hey1 in Xenopus and mouse. , Van Wayenbergh R ., Dev Dyn. December 1, 2003; 228 (4): 716-25.
The beta-catenin/ VegT-regulated early zygotic gene Xnr5 is a direct target of SOX3 regulation. , Zhang C., Development. December 1, 2003; 130 (23): 5609-24.
Control of embryonic Xenopus morphogenesis by a Ral-GDS/Xral branch of the Ras signalling pathway. , Lebreton S., J Cell Sci. November 15, 2003; 116 (Pt 22): 4651-62.
Xenopus autosomal recessive hypercholesterolemia protein couples lipoprotein receptors with the AP-2 complex in oocytes and embryos and is required for vitellogenesis. , Zhou Y., J Biol Chem. November 7, 2003; 278 (45): 44584-92.
Cardiac T-box factor Tbx20 directly interacts with Nkx2-5, GATA4, and GATA5 in regulation of gene expression in the developing heart. , Stennard FA ., Dev Biol. October 15, 2003; 262 (2): 206-24.
Endogenous Cerberus activity is required for anterior head specification in Xenopus. , Silva AC ., Development. October 1, 2003; 130 (20): 4943-53.
Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos. , Galli A., Development. October 1, 2003; 130 (20): 4919-29.
Fusicoccin signaling reveals 14-3-3 protein function as a novel step in left- right patterning during amphibian embryogenesis. , Bunney TD., Development. October 1, 2003; 130 (20): 4847-58.
Regulation of apoptosis in theXenopus embryo by Bix3. , Trindade M., Development. October 1, 2003; 130 (19): 4611-22.
XMAP215, XKCM1, NuMA, and cytoplasmic dynein are required for the assembly and organization of the transient microtubule array during the maturation of Xenopus oocytes. , Becker BE., Dev Biol. September 15, 2003; 261 (2): 488-505.
Calcium transients triggered by planar signals induce the expression of ZIC3 gene during neural induction in Xenopus. , Leclerc C ., Dev Biol. September 15, 2003; 261 (2): 381-90.
XMam1, the Xenopus homologue of mastermind, is essential to primary neurogenesis in Xenopus laevis embryos. , Katada T., Int J Dev Biol. September 1, 2003; 47 (6): 397-404.
Xenopus nucleosome assembly protein becomes tissue-restricted during development and can alter the expression of specific genes. , Steer WM., Mech Dev. September 1, 2003; 120 (9): 1045-57.
Pygopus is required for embryonic brain patterning in Xenopus. , Lake BB., Dev Biol. September 1, 2003; 261 (1): 132-48.
Wise, a context-dependent activator and inhibitor of Wnt signalling. , Itasaki N., Development. September 1, 2003; 130 (18): 4295-305.
The pro-BMP activity of Twisted gastrulation is independent of BMP binding. , Oelgeschläger M ., Development. September 1, 2003; 130 (17): 4047-56.